MAGNETOM Avanto Fit
K号: K190757 · 2019-05-31
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器械摘要
MAGNETOM Avanto Fit is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solution USA, Inc.. It received FDA 510(k) clearance on 2019-05-31 under 510(k) number K190757. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the MAGNETOM Avanto Fit?
MAGNETOM Avanto Fit is a medical device that received FDA 510(k) clearance on 2019-05-31. The listed applicant is Siemens Medical Solution USA, Inc.. The 510(k) number is K190757.
When did MAGNETOM Avanto Fit receive FDA 510(k) clearance?
MAGNETOM Avanto Fit received FDA 510(k) clearance on 2019-05-31, under 510(k) number K190757.
Who is the listed applicant for MAGNETOM Avanto Fit?
The FDA 510(k) record lists Siemens Medical Solution USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MAGNETOM Avanto Fit?
The FDA product code for MAGNETOM Avanto Fit is LNH.
相关临床试验
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列明Siemens Medical Solution USA, Inc.为申报人的其他记录
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
相关器械（代码：LNH）
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
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官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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